Related Experiment Video
Updated: Aug 21, 2025

08:03
Study of Protein Dynamics via Neutron Spin Echo Spectroscopy
Published on: April 13, 2022
2.2K
Proteinaceous microstructure in a capillary: a study of non-linear bending dynamics
Mario Marini1, Amirbahador Zeynali1, Maddalena Collini1,2
1Dipartimento di Fisica, Università degli Studi di Milano-Bicocca, Piazza della Scienza 3, 20126, Milano, Italy. giuseppe.chirico@unimib.it.
Lab on a Chip
|November 16, 2022
Summary
Researchers fabricated microstructures and studied their bending dynamics under fluid flow. Soft microstructures exhibited undamped oscillations, suggesting potential for energy conversion platforms.
Area of Science:
- Microfluidics
- Biomaterials Science
- Soft Matter Physics
Background:
- Flapping of flexible structures under flow is crucial in energy harvesting and microfluidic mixing.
- Microscale bending dynamics of such structures remain under-investigated.
- Understanding these dynamics is key for developing novel micro-devices.
Purpose of the Study:
- To fabricate and characterize the bending dynamics of microscale flexible structures.
- To investigate the influence of material properties and cross-sectional geometry on dynamics.
- To explore potential applications in energy conversion.
Main Methods:
- Two-photon laser polymerization for fabricating proteinaceous microstructures within micro-capillaries.
- Atomic Force Microscopy for testing elastic properties.
- Microfluidic experiments at intermediate Reynolds numbers (Re ≲ 150) to study deflection-flow dependence.
Main Results:
- Fabricated microstructures with Young's modulus (100 kPa ≤ E ≤ 4 MPa) comparable to biological tissues.
- Elastic constants (0.8 nN μm⁻¹ ≤ k ≤ 50 nN μm⁻¹) align with Euler Bernoulli theory.
- Soft microstructures (k ≤ 8 nN μm⁻¹) showed undamped bending oscillations (~10% deflection) due to viscoelasticity and non-linear dynamics.
Conclusions:
- Microstructure bending dynamics are tunable via laser fabrication intensity.
- Undamped oscillations in soft microstructures reveal complex fluid-structure interactions.
- These findings pave the way for developing novel energy conversion nanoplatforms.
Related Concept Videos
Mechanisms of Membrane-bending
2.7K
The living membranes are flexible due to their fluid mosaic nature; however, their bending into different shapes is an active process regulated by specific lipids and proteins. The membrane bending can be transient as seen in vesicles or stable for a long time as in microvilli. Cells regulate the size, location, and duration of the membrane curvature.
Membrane bending can happen due to intrinsic changes in lipid composition or extrinsic association with different proteins. The proteins involved...
Membrane bending can happen due to intrinsic changes in lipid composition or extrinsic association with different proteins. The proteins involved...
2.7K
Studying the Cytoskeleton
6.4K
The cytoskeletal architecture can be studied using different microscopic and biochemical techniques. Electron microscopy was instrumental in discovering the cytoskeletal architecture around the 1960s, which allowed obtaining structural information at a high-resolution level. However, the sample preparation procedure often limits this ability in biological samples. Several protocols have been developed over the years to optimize sample preparation. In one of the protocols known as rotary...
6.4K
Protein Dynamics in Living Cells
2.2K
Different fluorescence-based techniques are used to study the protein dynamics in living cells. These techniques include FRAP, FRET, and PET.
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...
2.2K

